Browse > Article
http://dx.doi.org/10.14402/jkamprs.2013.35.1.025

Changes of Compound Muscle Action Potential in Short-term Steroid Therapy for Compression Injury of Rat Sciatic Nerve  

Kim, So-Hyun (Department of Dentistry, Busan Paik Hospital, Inje University College of Medicine)
Park, Kwang-Won (Department of Dentistry, Busan Paik Hospital, Inje University College of Medicine)
Baek, Joon-Seok (Department of Dentistry, Busan Paik Hospital, Inje University College of Medicine)
Jung, Tae-Young (Department of Dentistry, Busan Paik Hospital, Inje University College of Medicine)
Kim, Mee-Lee (Department of Dentistry, Busan Paik Hospital, Inje University College of Medicine)
Park, Sang-Jun (Department of Dentistry, Busan Paik Hospital, Inje University College of Medicine)
Publication Information
Maxillofacial Plastic and Reconstructive Surgery / v.35, no.1, 2013 , pp. 25-30 More about this Journal
Abstract
Purpose: Many surgical procedures in oral and maxillofacial area can induce trauma to the peripheral nerve. The aim of the study is to evaluate the effects of short-term steroid therapy on nerve recovery after crush injury. Methods: Sixteen rats were randomly divided into two groups. The right sciatic nerves were exposed, crushed, and sutured. The control group was not given steroids. The test group was injected with dexamethasone disodium phosphate (2 mg/kg body weight/day) for 7 days. In all animals, compound muscle action potential (CMAP) was recorded before and at 1, 7, 14, 21, and 28 days after injury. Results: The amplitude of the CMAP before and at 1, 7, 14, 21, and 28 days after injury were $53.20{\pm}4.80$ mV, $20.12{\pm}5.38$ mV, $30.01{\pm}14.15$ mV, $31.14{\pm}13.56$ mV, $31.73{\pm}16.33$ mV, and $37.23{\pm}16.98$ mV in the control group, and $55.25{\pm}6.72$ mV, $18.62{\pm}6.26$ mV, $29.50{\pm}13.06$ mV, $32.90{\pm}13.226$ mV, $30.17{\pm}11.80$ mV, and $38.41{\pm}12.27$ mV in the test group, respectively. The nerve conduction velocity was $18.82{\pm}3.94$ m/s, $16.73{\pm}3.48$ m/s, $19.60{\pm}2.45$ m/s, $18.68{\pm}3.94$ m/s, $18.02{\pm}3.51$ m/s, and $19.25{\pm}3.88$ m/s in the control group, and $18.94{\pm}3.48$ m/s, $17.28{\pm}2.53$ m/s, $7.57{\pm}2.54$ m/s, $18.77{\pm}2.12$ m/s, $19.48{\pm}1.55$ m/s, and $19.22{\pm}2.97$ m/s in the test group, respectively. There was no significant difference between both groups (P>0.05). Conclusion: This study did not show any therapeutic effect of short-term administration of steroids on injured rat sciatic nerve. Further studies are needed.
Keywords
Nerve injury; Steroid; Compound muscle action potential;
Citations & Related Records
연도 인용수 순위
  • Reference
1 Miloro M. Microneurosurgery. In: Miloro M, Ghali GE, Peterson LJ, Larsen PE, Waite PD, editors. Peterson's principles of oral and maxillofacial surgery. 2nd ed. London: BC Decker Inc; 2004. p.819-37.
2 Seddon HJ. Three types of nerve injury. Brain 1943;66:237-88.   DOI
3 Sunderland S. A classification of peripheral nerve injuries producing loss of function. Brain 1951;74:491-516.   DOI   ScienceOn
4 Bleasel AF, Tuck RR. Variability of repeated nerve conduction studies. Electroencephalogr Clin Neurophysiol 1991;81:417-20.   DOI   ScienceOn
5 Lee KY, Kim WK, Kwon SH, et al. The usefulness of stand ardization of the nerve conduction study in the diagnosis and follow up of the demyelinating polyneuropathy. J Korean Neurol Assoc 1998;16:510-8.
6 Kimura J. Principles and pitfalls of nerve conduction studies. Ann Neurol 1984;16:415-29.   DOI   ScienceOn
7 Hong SL, Levine L. Inhibition of arachidonic acid release from cells as the biochemical action of anti-inflammatory corticosteroids. Proc Natl Acad Sci U S A 1976;73:1730-4.   DOI   ScienceOn
8 Schaberg SJ, Stuller CB, Edwards SM. Effect of methylprednisolone on swelling after orthognathic surgery. J Oral Maxillofac Surg 1984;42:356-61.   DOI
9 Blackwell GJ, Carnuccio R, Di Rosa M, et al. Glucocorticoids induce the formation and release of anti-inflammatory and anti-phospholipase proteins into the peritoneal cavity of the rat. Br J Pharmacol 1982;76:185-94.   DOI   ScienceOn
10 Tam S, Hong SC, Levine L. Relationships, among the steroids, of anti-inflammatory properties and inhibition of prostaglandin production and arachidonic acid release by transformed mouse fibroblasts. J Pharmacol Exp Ther 1977;203:162-8.
11 Seo K, Tanaka Y, Terumitsu M, Someya G. Efficacy of steroid treatment for sensory impairment after orthognathic surgery. J Oral Maxillofac Surg 2004;62:1193-7.   DOI   ScienceOn
12 Assimes TL, Lessard ML. The use of perioperative corticosteroids in craniomaxillofacial surgery. Plast Reconstr Surg 1999;103:313-21.   DOI
13 Fast A, Alon M, Weiss S, Zer-Aviv FR. Avascular necrosis of bone following short-term dexamethasone therapy for brainedema. Case report. J Neurosurg 1984;61:983-5.   DOI
14 Gibson N, Ferguson JW. Steroid cover for dental patients on long-term steroid medication: proposed clinical guidelines based upon a critical review of the literature. Br Dent J 2004;197:681-5.   DOI   ScienceOn
15 Durmus M, Karaaslan E, Ozturk E, et al. The effects of single- dose dexamethasone on wound healing in rats. Anesth Analg 2003;97:1377-80.
16 Sirois F. Steroid psychosis: a review. Gen Hosp Psychiatry 2003;25:27-33.   DOI   ScienceOn
17 Bracken MB, Shepard MJ, Collins WF Jr, et al. Methylprednisolone or naloxone treatment after acute spinal cord injury: 1-year follow-up data. Results of the second National Acute Spinal Cord Injury Study. J Neurosurg 1992;76:23-31.   DOI
18 Naso WB, Perot PL Jr, Cox RD. The neuroprotective effect of high-dose methylprednisolone in rat spinal cord hemisection. Neurosci Lett 1995;189:176-8.   DOI   ScienceOn
19 Hall ED. Neuroprotective actions of glucocorticoid and nonglucocorticoid steroids in acute neuronal injury. Cell Mol Neurobiol 1993;13:415-32.   DOI   ScienceOn
20 Chen A, Xu XM, Kleitman N, Bunge MB. Methylprednisolone administration improves axonal regeneration into Schwann cell grafts in transected adult rat thoracic spinal cord. Exp Neurol 1996;138:261-76.   DOI   ScienceOn
21 Lew H, Lee SY, Jang JW, Kim HY, Kang SJ, Kim SJ. The effects of high-dose corticosteroid therapy on optic nerve head blood flow in experimental traumatic optic neuropathy. Ophthalmic Res 1999;31:463-70.   DOI   ScienceOn
22 Galloway EB 3rd, Jensen RL, Dailey AT, Thompson BG, Shelton C. Role of topical steroids in reducing dysfunction after nerve injury. Laryngoscope 2000;110:1907-10.   DOI   ScienceOn
23 Nasser RM, Chen LE, Seaber AV, Urbaniak JR. Protective effect of 21-aminosteroid pretreatment in peripheral nerve low-load crush injury in mature and immature rats. J Orthop Res 1996;14:823-9.   DOI   ScienceOn
24 Al-Bishri A, Dahlin L, Sunzel B, Rosenquist J. Systemic betamethasone accelerates functional recovery after a crush injury to rat sciatic nerve. J Oral Maxillofac Surg 2005;63:973-7.   DOI   ScienceOn
25 Koyanagi I, Tator CH. Effect of a single huge dose of methylprednisolone on blood flow, evoked potentials, and histology after acute spinal cord injury in the rat. Neurol Res 1997;19:289-99.   DOI
26 Rabchevsky AG, Fugaccia I, Sullivan PG, Blades DA, Scheff SW. Efficacy of methylprednisolone therapy for the injured rat spinal cord. J Neurosci Res 2002;68:7-18.   DOI   ScienceOn
27 Lieberman DM, Jan TA, Ahmad SO, Most SP. Effects of corticosteroids on functional recovery and neuron survival after facial nerve injury in mice. Arch Facial Plast Surg 2011;13:117-24.
28 Hall ED, Springer JE. Neuroprotection and acute spinal cord injury: a reappraisal. NeuroRx 2004;1:80-100.   DOI   ScienceOn